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» Perfuse’s PER-001 intravitreal implant receives FDA clearance for first-in-human study in glaucoma
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Ocular
Perfuse’s PER-001 intravitreal implant receives FDA clearance for first-in-human study in glaucoma
April 5, 2023
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Perfuse Therapeutics Inc. has received FDA approval of its IND application for a first-in-human phase I/IIa study of PER-001 intravitreal implant in patients with glaucoma.
BioWorld Science
Ocular
FDA
IND
